Regulatory Affairs Internship — Medical Devices (EN/FR)

Jobtailor; Paris; Sur place; EUR 18 000 - 24 000; Plein temps

Résumé du poste

Jobtailor is seeking a Regulatory Affairs intern in France to support documentation, regulatory submissions, and automated watch processes. You will coordinate with multiple internal teams to ensure timely regulatory activities and license renewals for the US market.

You will assist with marketing/clinical claims review and post-market compliance, gaining exposure to quality/regulatory affairs in medical devices.

Qualifications

• Knowledge of medical devices and related regulations.
• Familiar with regulatory submissions and post-market activities.
• Experience with regulatory quality processes is a plus.

Responsabilités

• Monitor and ensure timely preparation and tracking of technical documentation for design changes.
• Assist in documentation preparation and publishing for regulatory submissions.
• Assist in implementing an automated regulatory watch system.
• Monitor renewal of licenses for US market (SB Determination, Device Listing, Establishment License).
• Support centralized database for marketing and clinical claims review.
• Perform regulatory watch to ensure compliance with FDA, ISO, and other standards.
• Provide support for post-market compliance activities.

Connaissances

Medical devices knowledge

Software medical devices experience

Regulatory affairs experience

Formation

Bac+5 Master’s degree (Regulatory Affairs, or related field)

Description du poste

Jobtailor is seeking a Regulatory Affairs intern in France to support documentation, regulatory submissions, and automated watch processes. You will coordinate with multiple internal teams to ensure timely regulatory activities and license renewals for the US market.

You will assist with marketing/clinical claims review and post-market compliance, gaining exposure to quality/regulatory affairs in medical devices.